Skip to main content
Log in

Initiating factors in perineuronal cell hyperplasia associated with chromatolytic neurons

  • Published:
Zeitschrift für Zellforschung und Mikroskopische Anatomie Aims and scope Submit manuscript

Summary

Neuronal hypertrophy and increased metabolism in nerve cells are evaluated as possible factors initiating hyperplasia of perineuronal cells. Colchicine induced neuropathy in the dorsal root ganglia is used as the model of increased neuronal metabolism.

Twenty-eight female white rats weighing 100 g were divided into four groups, each animal receiving a 50 μl injection into the subarachnoid space at the lumbosacral level eight days and again three days before sacrifice. The 50 μl contained 25, 2.5 and 0.25 μg of colchicine in distilled water for the first three groups and normal saline for the last group.

A Zeiss ocular with random test points was used to determine the volume of tissue occupied by perineuronal cells and nerve cells in spinal ganglia. Direct cell counts yielded the size of the population of perineuronal cells and neurons.

Irreversible motor and sensory loss occurred with the high dose injection, reversible loss with the 2.5 μg injection and no loss with either the low dose or the saline injection. Chromatolytic neurons were noted in all animals receiving colchicine. Neither proliferation of perineuronal cells nor neuronal hypertrophy were observed. Neuronal hypertrophy, rather than altered neuronal metabolism, may be the initiating event in the perineuronal cell hyperplasia that frequently accompanies chromatolysis.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Bodian, D., Mellors, R. C.: The regenerative cycle of motor neurons with special reference to phosphatase activity. J. exp. Med. 81, 469–487 (1945).

    Google Scholar 

  • Brattgård, S. O., Edström, J. E., Hyden, H.: The chemical changes in regenerating neurons. J. Neurochem. 1, 316–325 (1957).

    Google Scholar 

  • Carmel, P. W., Stein, B. M.: Cell changes in sensory ganglia following proximal and distal nerve section in the monkey. J. comp. Neurol. 135, 145–165 (1969).

    Google Scholar 

  • Edström, J. E.: Ribonucleic acid changes in the motoneurons of the frog during axon regeneration. J. Neurochem. 5, 43–49 (1959).

    Google Scholar 

  • Embree, L. J., Hamberger, A., Sjöstrand, J.: Quantitative cytochemical studies and histochemistry in experimental neurofibrillary degeneration. J. Neuropath. exp. Neurol. 26, 427–436 (1967).

    Google Scholar 

  • Friede, R. L., Johnstone, M. A.: Response of thymidine labeling of nuclei in gray matter and nerve following sciatic transection. Acta neuropath. (Berl.) 7, 218–231 (1967).

    Google Scholar 

  • Hamberger, A.: Difference between isolated neuronal and vascular glia with respect to respiratory activity. Acta physiol. scand. 58, Suppl. 203, 1–58 (1963).

    Google Scholar 

  • —, Sjöstrand, J.: Respiratory enzyme activities in neurons and glial cells of the hypoglossal nucleus during nerve regeneration. Acta physiol. scand. 67, 76–88 (1966).

    Google Scholar 

  • Hugosson, R., Källen, B., Nilsson, O.: Neuroglia proliferation studied in tissue culture. Acta neuropath. (Berl.) 11, 210–220 (1968).

    Google Scholar 

  • Humbertson, A., Zimmerman, E., Leedy, M.: A chronological study of mitotic activity in satellite cell hyperplasia associated with chromatolytic neurons. Z. Zellforsch. 100, 507–515 (1969).

    Google Scholar 

  • Klatzo, I., Wisniewski, H., Streicher, E.: Experimental production of neurofibrillary degeneration. I. Light microscopic observations. J. Neuropath. exp. Neurol. 24, 187–199 (1965).

    Google Scholar 

  • Konigsmark, B. W., Sidman, R. L.: Origin of brain macrophages in the mouse. J. Neuropath. Exp. Neurol. 22, 643–676 (1963).

    Google Scholar 

  • Kreutzberg, G. W.: Changes of coenzyme (TPN) diaphorase and TPN-linked dehydrogenase during axonal reaction of the nerve cell. Nature (Lond.) 199, 393–394 (1963).

    Google Scholar 

  • Pannese, E.: Investigations on the ultrastructural changes of the spinal ganglion neurons in the course of axon regeneration and neuronal hypertrophy. I. Changes during axon regeneration. Z. Zellforsch. 60, 711–740 (1963a).

    Google Scholar 

  • —: Investigations on the ultrastructural changes of the spinal ganglion neurons in the course of axon regeneration and neuron hypertrophy. II. Changes during cell hypertrophy and comparison between the ultrastructure of nerve cells of the same type under different functional conditions. Z. Zellforsch. 61, 561–585 (1963b).

    Google Scholar 

  • —: Number and structure of perisomatic satellite cells of spinal ganglia under normal conditions or during axon regeneration and cell hypertrophy. Z.Zellforsch. 63, 568–592 (1964).

    Google Scholar 

  • Peterson, E., Murray, M.: Serial observations in tissue cultures on neurotoxic effects of colchicine. Anat. Rec. 154, 401 (1966).

    Google Scholar 

  • Schwyn, R. C.: An autoradiographic study of satellite cells in autonomic ganglia. Amer. J. Anat. 121, 727–740 (1967).

    Google Scholar 

  • Sjöstrand, J.: DNA synthesis in glial cells during nerve regeneration. Experientia (Basel) 21, 142–143 (1965).

    Google Scholar 

  • —: Glial cells in the hypoglossal nucleus of the rabbit during nerve regeneration. Acta physiol. scand. 67, Suppl. 270, 1–43 (1966).

    Google Scholar 

  • Smith, M. L., Adrian, E. K.: Infiltration of prelabeled mononuclear cells into dorsal root ganglia following transection of the sciatic nerve. Anat. Rec. 166, 380 (1970).

    Google Scholar 

  • Terry, R. D., Pena, C.: Experimental production of neurofibrillary degeneration. II. Electron microscopy, phosphatase histochemistry and electron probe analysis. J. Neuropath. exp. Neurol. 24, 200–210 (1965).

    Google Scholar 

  • Torvik, A., Heding, A.: Histological studies on the effects of actinomycin D on retrograde nerve cell reaction in the facial nucleus of mice. Acta neuropath. (Berl.) 9, 146–157 (1967).

    Google Scholar 

  • —: Effect of actinomycin D on retrograde nerve cell reaction further observations. Acta neuropath. (Berl.) 14, 62–71 (1969).

    Google Scholar 

  • Watson, W. E.: An autoradiographic study of the incorporation of nucleic-acid precursors by neurones and glia during nerve regeneration. J. Physiol. (Lond.) 180, 741–753 (1965a).

    Google Scholar 

  • —: An autoradiographic study of the incorporation of nucleic-acid precursors by neurones and glia during nerve stimulation. J. Physiol. (Lond.) 180, 754–765 (1965b).

    Google Scholar 

  • Wisniewski, H., Terry, R. D.: Experimental colchicine encephalopathy. I. Induction of neurofibrillary degeneration. Lab. Invest. 17, 577–587 (1967).

    Google Scholar 

  • —, Shelanski, M. L., Terry, R. D.: Effects of mitotic spindle inhibitors on neurotubules and neurofilaments in anterior horn cells. J. Cell Biol. 38, 224–229 (1968).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zimmerman, E., Karsh, D. & Humbertson, A. Initiating factors in perineuronal cell hyperplasia associated with chromatolytic neurons. Z. Zellforsch. 114, 73–82 (1971). https://doi.org/10.1007/BF00339466

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00339466

Key-Words

Navigation